A Novel CCK Receptor GPR173 Mediates Potentiation of GABAergic Inhibition

Cholecystokinin (CCK) enables excitatory circuit long-term potentiation (LTP). Here, we investigated its involvement in the enhancement of inhibitory synapses. Activation of GABA neurons suppressed neuronal responses in the neocortex to a forthcoming auditory stimulus in mice of both sexes. High-frequency laser stimulation (HFLS) of GABAergic neurons potentiated this suppression. HFLS of CCK interneurons could induce the LTP of their inhibition toward pyramidal neurons. This potentiation was abolished in CCK knock-out mice but intact in mice with both CCK1R and 2R knockout of both sexes. Next, we combined bioinformatics analysis, multiple unbiased cell-based assays, and histology examinations to identify a novel CCK receptor, GPR173. We propose GPR173 as CCK3R, which mediates the relationship between cortical CCK interneuron signaling and inhibitory LTP in the mice of either sex. Thus, GPR173 might represent a promising therapeutic target for brain disorders related to excitation and inhibition imbalance in the cortex. SIGNIFICANCE STATEMENT CCK, the most abundant and widely distributed neuropeptide in the CNS, colocalizes with many neurotransmitters and modulators. GABA is one of the important inhibitory neurotransmitters, and much evidence shows that CCK may be involved in modulating GABA signaling in many brain areas. However, the role of CCK-GABA neurons in the cortical microcircuits is still unclear. We identified a novel CCK receptor, GPR173, localized in the CCK-GABA synapses and mediated the enhancement of the GABA inhibition effect, which might represent a promising therapeutic target for brain disorders related to excitation and inhibition imbalance in the cortex.

CCK-related inhibitory plasticity has been characterized by the aspects of brain regions, cell types, and synapses. CCK-mediated inhibitory plasticity requires high-frequency stimulation (HFS) as well as CCK2R activation and astrocytic ATP release in the dorsomedial hypothalamus via increased GABA release (Crosby et al., 2015(Crosby et al., , 2018. CCK increases the frequency of spontaneous ISPCs (sIPSPs) and currents (sIPSCs) in the basolateral amygdala (Chung and Moore, 2007). Recently, Martinez Damonte et al. (2022) reported that HFS-induced somatodendritic-released CCK potentiates GABAergic synapses onto ventral tegmental area dopamine cells. Also, Dudok et al. (2021) found that CCK basket cell activity inversely scales with pyramidal cell ensemble activity during locomotion and rest. However, cortical CCK-IN-induced iLTP is not fully elucidated at the presynaptic or postsynaptic levels. Despite CCK being a marker for cortical GABAergic neurons (Kubota and Kawaguchi, 1997), its functional role in cortical GABA inhibitory synapses is still unknown, as well as which CCK receptor is involved in this process.
CCK1R and CCK2R, two known CCK receptors in the mammalian brain (Moran et al., 1986;Wank et al., 1992;Noble and Roques, 1999), are G-protein-coupled receptors (GPCRs). CCK1R links hippocampal LTP and spatial memory (Harro and Oreland, 1993). CCK2R mediates LTP in excitatory synapses and enables associative memory encoding between two sounds, sound and light, or sound and fear (Li et al., 2014;Chen et al., 2019;Zhang et al., 2020;Feng et al., 2021). Given that CCK mediates excitatory and inhibitory circuit LTP in different brain regions, the following question arises: Does CCK released from GABAergic neurons mediate iLTP in the cortex via known CCK receptors?
We performed in vivo extracellular and in vitro patch-clamp recording experiments to address the above question in the present study. We found that iLTP was not induced in CCK-KO mice but in CCK1R/2R double KO mice, implying that a novel CCK receptor mediates iLTP. Our next objective was to identify this novel CCK receptor. We then screened the homology and similarities of known GPCRs to CCK1R and CCK2R using a bioinformatics algorithm to shortlist candidate receptors, followed by multiple cell-based assays to validate their binding properties with the CCK ligand. We also examined the colocalization of candidate GPCRs and CCK-GABAergic synapses and their distribution in excitatory and inhibitory neurons. Finally, we performed loss-of-function studies in cell and brain slice assays. In this manner, we identified GPR173 as a novel CCK receptor involved in the iLTP of CCK-INs in the cortex.
Optogenetics: in vivo local field potential and unit recordings In vivo recordings. We performed in vivo recordings 3-4 weeks after virus injection, as previously described (Li et al., 2014;Chen et al., 2019;Zhang et al., 2020). We injected mice with atropine to inhibit tracheal secretions 15 min before urethane sodium anesthetic injection (2 Â g/kg, i.p.; Sigma-Aldrich. We performed a craniotomy to access the AC (À1.8 to À3.5 mm posterior to bregma and À3.5 to À4.5 mm to the midline).  (Table continues) We inserted a recording borosilicate glass (World Precision Instruments) electrode array (pulled with a Sutter-87 puller) 300-500 mm deep. We placed a laser fiber (200-mm diameter, RWD Life Science) on the surface of the AC where the virus was infused. We controlled a stepping-motor microdriver outside the soundproofed chamber to advance the electrode array. Signals were preamplified, filtered with a bandwidth of 1-5000 Hz, and stored in a Tucker-Davis Technologies (TDT) workstation (OpenEx). The TDT workstation generated a noise burst of 100 ms duration that led to a coupled electrostatic speaker as the auditory stimulus [AS; 50-105 dB, sound pressure level (SPL)]. When the AS reached the animal, a condenser microphone was used to measure and adjust the sound intensity of the speaker (Center Technology). A laser generator (Newdoon) delivered a laser pulse (5 ms duration) at a 473 nM wavelength. We set the intensity of the laser at ;0-10 mW at the end of the laser fiber.
We measured the input-output curve between the sound intensity (60-95 dB, SPL) and the amplitude of the local field potential (LFP). We adopted the intensity that evoked 50% of the maximum response as the sound intensity. We also measured the input-output curve between the laser power (0-15 mW) and the amplitude of the LFP to help select the laser power. We adopted the laser power that evoked 50-70% of the maximum response as the stimulation power in every experiment.
We confirmed viral expression by examining the laser-induced suppressive effect on spontaneous neuronal responses. We selected the interval between the laser and AS to achieve the optimal suppressive effect of laser-activated inhibitory neurons on neuronal responses to the forthcoming AS. We set a gap of 50 ms for subsequent experiments. The LFP traces were calculated with MATLAB and plotted over time.
We examined spontaneous neuronal activities and responses to the laser and AS combination as units and LFP (0.1 Hz) for 15 min. We delivered a single-pulse laser (3-5 mW, 5 ms duration) in 0.1 Hz repetitions 50 ms before the AS. We recorded for 15 min before (baseline) and 60 min after high-frequency laser stimulation (HFLS; 5 pulses at 40 Hz, repeated for 40 trials at 0.1 Hz). We examined the frequency of HFLS as a parameter to confirm laser-evoked responses, which helped us select the laser frequency as our desired HFLS and remove light/heat effects (1-120 Hz, repeated for 20 trials at 0.1 Hz).
In vivo LFP analysis. We averaged LFP amplitudes across every six trials (MATLAB), representing a 1 min recording, and plotted the representative waveforms with MATLAB.
We present group data as the mean 6 SEM. We used 3-11 mice per condition for each experiment. We randomly selected male or female mice for each experiment. For all in vivo electrophysiology experiments, n refers to the number of recording sites per condition, and N refers to the number of animals. We analyzed data in a blinded manner. We performed a two-way ANOVA and Tukey's post hoc tests for experiments involving two independent variables using IBM SPSS Statistics software or Microsoft Excel, assuming a normal distribution when n was too small to determine distribution. We used OriginPro 8.5 software to show group data in all figures.
Unit waveform processing. We used commercial hardware and software (OpenEx) to analyze the waveform from every unit with OpenBridge, Plexon Offline Sorter, and NeuroExplorer. We recorded multiunits primarily with the current electrode preparation.
We discriminated units from the PLX file using principal component analysis with the Plexon Offline Sorter. We adopted two criteria to ensure the quality of recorded units, (1) a signal larger than three times the noise band and (2) no more than 1% of the interspike intervals shorter than 2 ms. We considered only those neurons with at least 1000 detected spikes within 15 min in our analysis.
We opened the sorting in the NEX5 file by NeuroExplorer. We plotted rasters and histograms for units using perievent rasters with specific, fixed reference events (laser, AS, or sweep) with a 5 ms bin width. We extracted the single and averaged waveforms into OriginPro 8.5. Counts per bin (5 ms) depending on the duration of the fixed reference event time for a comparable experiment were used for firing rate quantification. We calculated the average firing rate during the 100 ms AS presentation. We excluded the period between the laser and 100 ms after the AS presentation from the spontaneous firing rate quantification because such firing corresponded to the indirect activation of GABAergic neurons or a delayed noise response.
Whole-cell recordings. We performed whole-cell recordings with a MultiClamp 700B amplifier and Digital 1440A digitizer (Molecular Devices) targeting the AC in the brain slices in room temperature aCSF containing the following (in mM): 119 NaCl, 2.5 KCl, 1.25 NaH 2 PO 4 , 24 NaHCO 3 , 12.5 glucose, 2 CaCl 2 ·4H 2 O, and 2 MgSO 4 ·7H 2 O, ;25°C). We pulled patch pipettes with resistance between 3 and 5 MV from borosilicate glass (World Precision Instruments) on a Sutter-87 puller. The intracellular solution contained the following (in mM): 145 K-Gluconate, 10 HEPES, 1 EGTA, 2 Mg-ATP, 0.3 Na 2 -GTP, and 2 MgCl 2 , pH 7.3, 290-300 mOsm. We made recordings after giga-ohm seal formation and terminated if Rs changed .20%. We selected pyramidal neurons (PC) based on their pyramidal-like shape and their regular spiking firing pattern by injecting step currents. We infused Biotin Alexa Fluor 488 after recording to confirm the patched pyramidal neuron. We applied laser stimulation through an optical fiber placed ;200 mm from the recording neuron using Aurora-220 (473 nm, Newdoon) to activate ChR2 1 neurons (GABAergic). We selected neurons that responded to the laser pulse only in our experiment. We delivered HFLS (10-pulse burst at 40 Hz, repeated for 10 trials) or low-frequency laser stimulation (LFLS; 1 Hz, 100 pulses) with a 15 s interval. We recorded IPSCs in response to the laser stimulation (1 pulse per 15 s, 5 ms in duration) under voltage-clamp recording mode (holding at À60 mV to À50 mV) for 5 min as the baseline before and for 25 min after HFLS or LFLS. In a subset of experiments, we applied 200 nM sulphated CCK8 (CCK8s) via bath application 3 min before LFLS. In another subset of experiments, we applied devazepide in the recording chamber via bath application (60 nM) 3 min before HFLS. Drugs were naturally washed out. For the normalization of recorded IPSCs in the CCK-Cre, PV-Cre, CCK-KO, and CCK1R/2R-KO mice, we selected only patched neurons with IPSCs .35 pA.
Searching for potential candidates of CCK receptors by bioinformatics methods Proteomics screening in the GPCR pool in comparison with CCK1R and CCK2R. We downloaded ;200 GPCRs, both orphans and characterized receptors, known from the literature as FASTA formatted sequences obtained from UniProt (https://www.uniprot.org). All FASTA formatted sequences were merged into one file for further analysis. For the hierarchical cluster and scores for CCK1R/2R, we set two parameters as follows: (1) We selected binding sites from the GPCRs secondary structure (extramembrane) based on the CCK binding domains of CCK1R and CCK2R, and (2) we compared amino acid sequences based on the hamming distance. After identifying all proteins with these two parameters, we selected GPCRs with high similarity scores for both CCK1R and CCK2R. We analyzed the data with the online free software NetSurfP version 1.1 (new version available at https://services.healthtech.dtu.dk/service. php?NetSurfP-1.1). NetSurfP predicts amino acid surface accessibility and secondary structure in an amino acid sequence. This study validated total similarity scores for CCK1R and CCK2R above 30 without additional manual inspection.
Percentage identity of CCK1R, CCK2R, and 79 orphan GPCRs. We examined the percentage identity matrix for 79 orphan GPCRs with CCK1R and CCK2R. Percentage identity is the quantitative correlation estimation between two sets of sequences. Closely correlated species have a higher percentage identity for a given amino acid sequence. Hence, percentage identity reflects relatedness to some extent. The sequences of 79 orphan GPCRs, together with CCK1R and CCK2R proteins, were analyzed and plotted by a customdesigned program.
Peptide synthesis. Peptides and modified peptides were chemically synthesized by Bankpeptide Biotechnology, Synpeptide, or Shanghai Ke Biochem. HPLC analysis results ensured that the purity of peptides was .97%. We list peptide and modified peptide sequences in Table 1.
Plasmid construction. For CHO-GPCR cell line construction, human coding sequences (CDSs) of the GPCRs were cloned into multiple cloning sites of pLVX-puro. For the cell surface binding assay, Flag (at the N terminus of GPCRs)-tagged human GPCR coding sequences were cloned into pCDNA3.1(1) plasmids. For the b -arrestin2 recruitment assay, our Tango-GPCR plasmids were constructed based on pCDNA3.1 (1) as described previously (Kroeze et al., 2015), except that we cloned the full CDS of human GPCRs into pCDNA3.1(1). For the b -arrestin1/ 2 recruitment assay, the b -arrestin1-linker-TEV (tobacco etch virus) protease-HA tag was cloned into pCDNA3.1(1), in which b -arrestin1 was the human CDS (NM_004041.5), TEV protease was the 2040-2279aa fragment of TEV Nla protease (accession #M15239.1, GenBank), and linker sequence was the (Gly 4 Ser) 2 coding sequence. All final recombinant vectors were confirmed by sequencing analysis.
Cell surface binding assay. We transfected HEK293T cells with pCDNA3.1(1)-Flag-GPCR (purchased from Public Protein/Plasmid Library or made in our laboratory based on a pCDNA3.1(1) backbone). We incubated the cells with HA-(« -Ahx) 2 (as a negative control) or HA-(« -Ahx) 2 -CCK8s dissolved in HHBS solution (including 20 mM HEPES, pH 7.4) for 30 min at room temperature 48 h after transfection by Lipo6000 (Beyotime Biotechnology). After three washes with HHBS, cells were fixed in 4% paraformaldehyde (PFA) and 4% sucrose in PBS for 15 min at room temperature. Cells were blocked in 5% normal goat serum in PBS, and staining was performed in detergent-free conditions without cell permeabilization after three washes by PBS. We used primary antibody rabbit anti-HA (catalog #8146, Cell Signaling Technology), anti-GPR173 (catalog #PA5-50 976, Thermo Fisher Scientific), and mouse anti-Flag (catalog #3724, Cell Signaling Technology) to detect HA and Flag tags. Images were captured on a Leica SP8 confocal microscope. Images within each experiment were collected using identical laser power, offset, and gain.
Immunohistochemical staining. For immunohistochemistry, we deeply anesthetized mice with an overdose of pentobarbital sodium. We transcardially perfused mice with 30 ml cold PBS and 30 ml 4% (w/v) PFA. Brain tissue was removed, postfixed with 4% PFA, and treated with 30% (w/v) sucrose in 4% PFA at 4°C for 2-3 d. Brain tissue was sectioned on a cryostat (30 mm for standard staining and 10 mm for super-resolution imaging; Leica CM3500) and preserved with antifreeze buffer (20% v/v glycerin and 30% v/v ethylene glycol diluted in PBS) at À20°C. For immunostaining and statistical analysis of colabeled neurons and axonal synapses in the AC, serial sections containing the AC were selected for analysis. Brain sections were rinsed three times with PBS and blocked with blocking buffer (10% v/v goat serum in PBS with 0.2% v/v Triton X-100) for 2 h at room temperature. Sections were incubated with primary antibodies (Table 1) at 4°C for 24-36 h. After washing four times in PBS (each time for 10 min), sections were incubated with the corresponding fluorophore-conjugated secondary antibodies (Table 1) for 2.5-3 h at 25°C. Sections were then rinsed with PBS three times before DAPI staining (1:5000 v/v diluted in PBS) or mounting. We mounted all sections with 70% v/v glycerin in PBS (standard staining) or imaging buffer (super-resolution imaging) on slides.
Image acquisition and analysis. Image acquisition (10Â, 20Â, 63Â, and 100Â magnification) was performed using a Nikon A1hD25 confocal microscope. The confocal microscope was equipped with a time delay integration camera and performed line scanning with fast acquisition at a high resolution of the fluorescent signal.
We took images at 20Â magnification and montaged them with the same laser settings between parallel studies. We optimized the gain and exposure parameters for each image. We captured Z-stacks throughout the tissue for magnified images showing labeling details. For quantification of colocalization, neurons expressing the indicated reporter were counted using only the corresponding color channel. Then, among these cells, the number of neurons coexpressing the marker of interest was counted by Nikon imaging analysis software (NIS-Elements Viewer 5.21). Bright spot detection was performed in the fields of interest in brain regions with the software under an appropriate fluorescent threshold. A neuron was positive for a given marker if the corresponding signal was above the background fluorescence. The ratio of neurons coexpressing both markers over the total number of cells expressing only the reporter was then calculated.
The n in the figures indicates the number of representative biological replicates, and N indicates the number of independent animals. At least three biological replicates per data point were included for all quantifications used in the present study.
Super-resolution imaging and processing. The staining process for super-resolution imaging was the same as immunohistochemical staining except for differences in secondary antibody and mounting. Two fluorophores were used (Alexa Fluor 647 in combination with Alexa Fluor 750) as secondary antibodies. To immobilize a labeled slice, we first applied 200 ml fluorescent beads (Thermo Fisher Scientific) onto the 1.5mm-thick cover glass with 120°C heating to attach tightly. After several washes with double-distilled H 2 O, a well-labeled slice of the AC was gently attached to the cover glass where beads were attached. After drying, the slice was sealed on the slide with imaging buffer (150 mM Tris, pH 8, 1% glycerol, 1% glucose, 10 mM NaCl, 1% b -Mercaptoethanol, 0.5 mg/ml glucose oxidase, 40 mg/ml catalase). We performed dSTORM imaging in a freshly prepared imaging buffer to slow the speed of fluorophores quenching during imaging acquisition. STORM imaging was performed on a 20Â and 100Â Olympus microscope [NanoBioImaging SRiS 2.0 (STORM) Super-Resolution Microscope, Hong Kong University, Olympus] and analyzed with ImageJ software (National Institutes of Health).
In super-resolution capture mode, we first locked slice focus with Narrow Band Imaging Rohdea 3.0 under 20Â magnification by capturing the signal of fluorescent beads attached to slides. A Z-stack of fluorescent beads at this moment acted as a reference. We first turned on a 405 nm laser to activate the two fluorophores. Under illumination at 10-15% of the maximum output power of 656 nm and 750 nm lasers, we observed a preview of the target signal before imaging. We acquired 3000 frames with 656 nm and 750 nm laser illumination at 30-50% maximum output power to activate the two fluorophores. We estimated drift using the inbuilt function in SRiS 2.0 and applied correction during analysis. The raw data, single-channel Excel file, and raw data files were autogenerated for analysis after capturing.
The Excel file was directly imported into ImageJ. After dataset reconstruction with the same parameters for both channels, red and green RGB (red, green, and blue) colors were used to differentiate the fluorophores in the two channels. The two colors were merged into one channel, forming the overlay images.
The Pearson correlation coefficient (PCC) and Manders' overlap coefficient (MOC) are common metrics for measuring the predictability of colocalization (Aaron et al., 2018). In more mathematical terms, the PCC can be thought of as the covariance between the two images, normalized by the product of their SDs.
Meanwhile, we seeded ;1 Â 10 6 CHO cells in six-well plates with 0.5 ml virus supernatant per well for 12 h and then mixed and added 0.1% polybrene (Sigma-Aldrich) in 1 ml fresh normal medium. We performed the second infection for 24 h and replaced the virus supernatant mix with a fresh normal medium of CHO after 6-8 h of each infection. Two days after the second infection, we added puromycin (Invitrogen) at a final concentration of 10 mg/ml for 1 week. To obtain high-expression cell lines, we isolated single cells by limited dilution in 96-well plates and performed quantitative RT-PCR (qRT-PCR) after 1 month of culture. Finally, the highest-expressing cell line was chosen for further characterization.
GPR173 knockdown with shRNA (Gpr173) in CHO-GPR173 cells. The coding sequence of Hygromycin B was PCR-amplified by Phanta Max Super-Fidelity DNA Polymerase (Vazyme Biotech) from other plasmids. The purified Hygromycin B fragment and pLKO.1-puro plasmid (catalog #8453, Addgene) was digested by BamHI and KpnI restriction enzyme (New England Bio Labs). We separated the resulting fragments by 1.0% agarose gel electrophoresis and retrieved them using a DNA retrieval kit (Tiangen Biotech). We combined the two BamHI and KpnI fragments with T4 DNA ligase (New England Bio Labs). We termed the generated plasmid "pLKO.1-hygro." We then designed and cloned the selected shRNA sequence into the pLKO.1-hygro plasmid by AgeI/ EcoRI sites. We determined the most effective shRNA (Gpr173) sequence, ACGTGGGCACCTACAAGTTTA (with scramble sequence as follows: CCTAAGGTTAAGTCGCCCTCG). We generated a GPR173 knock-down cell line using the method described above. After lentivirus infection of CHO-GPR173 cells, we screened cells with 400 mg/ml Hygromycin B (Thermo Fisher Scientific) for at least 1 week.
qRT-PCR. Primer synthesis was conducted by Generay Biotechnology using the following sequences: gpr173-TCTGGTCACCCTACATCGTG/ CAGTAGGGTTCTCTGGGAGC and actb-CCTCTATGCCAACACAG TGC/CCTGCTTGCTGATCCACATC. After extracting total RNA using an RNAsimple Total RNA Kit (TIANGEN Biotech), we used 1.6 mg RNA and a FastKing RT Kit (TIANGEN Biotech) to generate cDNA according to the instructions from the manufacturer. Then, the primers were amplified with SYBR Green Mix (TIANGEN Biotech) through the 2 ÀDCt method. The actb was used as an endogenous control gene for gpr173. We repeated all procedures three times in triplicate.
Ca 21 imaging assay. For Ca 21 mobilization by a confocal microscope, ;8 Â 10 4 transfected cells were seeded in each well of an eightwell chambered cover glass (Thermo Fisher Scientific) the day before the Ca 21 imaging assay. Then, 5 mM Fluo-8 (AAT Bioquest) dissolved in HHBS solution was incubated with the cells for 30 min in a cell incubator and 30 min at room temperature after removing the culture medium. These cells were washed three times with HHBS, and 360 ml HHBS was added. Subsequently, images of these cells were captured by a Zeiss 710 nonlinear optical confocal microscope before and after being treated with 10Â compounds or HHBS solution.
The Ca 21 imaging assay was performed using an EnVision 2104 Multilabel Reader (PerkinElmer; excitation, 485 nm and emission, 535 nm). A total of 6 Â 10 4 cells grown in each well overnight on a 96well optical-bottom plate with a cover glass base (Corning) were measured by a Fluo-8 No Wash Calcium Assay Kit (AAT Bioquest), which is the most effective dye for detecting intracellular free Ca 21 . Cells were cultured at 37°C, and 5% CO 2 in DMEM/F-12 medium (Thermo Fisher Scientific) containing 10% FBS (Natocor Industria Biológica) and washed with DMEM/F-12 medium once after overnight incubation.
b -arrestin recruitment assay. For the b -arrestin2 recruitment assay, a PRESTO-Tango assay was performed as described previously (Kroeze et al., 2015) with some modifications. HTLA cells (a HEK293 cell line stably expressing a tTA-dependent luciferase reporter and a b -arrestin2-TEV fusion gene; a gift from the laboratory of Richard Axel and Wang Sheng) grown in each well of a six-well plate were transfected with 1 mg GPCR CDS containing the Tango construct according to instructions from the manufacturer. The transfected cells were seeded in poly-L-lysine-coated 384-well plates (catalog #J03841, JingAn Biological) at 15,000-20,000 cells per well in 50 ml medium for 24 h. The medium was replaced by a fresh medium containing a series of concentrations of compounds after 24 h of culture in a 384-well plate. Medium and drug solutions were removed from each well after ;18 h of incubation with cells, and 20 ml per well of Bright-Glo solution (Promega) was diluted 20-fold in assay buffer (1Â HBSS, 2.5 mM probenecid, 20 mM HEPES, pH 7.4) and added to each well. After ;15 min of incubation at room temperature, luminescence was quantified in an EnVision 2104 Multilabel Reader (PerkinElmer) or FlexStation 3 system (Molecular Devices). The relative luminescence was exported into an Excel sheet and processed with Excel and GraphPad Prism 6 software. Procedures for the b -arrestin1/2 recruitment assay were the same, except that 0.5 mg b -arrestin1-expressing plasmid was transfected together with 1 mg Tango-GPCR plasmids into HTLA cells.

Quantification, statistical analysis, and reproducibility
We performed quantification using a minimum of three independent biological replicates. Data collection and analysis were not performed in a blinded manner if not specified, but different research groups performed the quantifications. We present group data as the mean 6 SEM. We used IBM SPSS 25.0 software and Microsoft Excel to perform statistical analyses, including Student's unpaired t tests, Student's paired t tests, one-way ANOVA with Tukey's post hoc tests, and two-way repeatedmeasures (RM) ANOVA with Tukey's HSD. Asterisks or number signs denote significant differences in all figures (*p , 0.05, *p , 0.01, ***p , 0.001, ****p , 0.0001, and ####p , 0.0001). N.S. indicates a nonsignificant difference. We used OriginPro 8.5 (OriginLab Corporation), Inkscape 0.92.3 (Inkscape), and GraphPad Prism 6 software to create graphs. The reference brain map with anatomic abbreviations is accessible on the Allen Brain Atlas website.

CCK-INs potentiate inhibition in the AC
We adopted an in vivo recording animal model for the first experiment. Considering activation of GABAergic neurons induces inhibitory outputs to nearby neurons in the neocortex, we assumed prior activation of GABAergic neurons would suppress neuronal responses in the AC to a forthcoming AS.
In the in vivo setup for anesthetized mice (Fig. 1C), normalized sound intensity, and laser power were selected after measuring the input-output curve of each mouse for stimulus intensities. Also, the kinetics of optogenetic opsin were examined by applying laser pulse trains of different frequencies (1-120 Hz) in both groups to ensure normal firing of GABAergic neurons after knocking out CCK.
Laser stimulation significantly suppressed evoked response to the forthcoming AS in ChETA-eYFP-injected Vgat-Cre mice (Fig. 1D, left), response to the AS in raster displays (90 trials over 15 min), and poststimulus histograms (PSTHs; bin width, 10 ms; middle, response to the AS preceded by laser stimulation; right, mean auditory response calculated in a 100 ms observation window starting 20 ms after the AS in ChETA-eYFP-injected mice, which was reduced from 152.23 6 29.22 to 104.07 6 20.75 Hz (n = 17 units; two-way ANOVA with Tukey's post hoc test, ***p , 0.001). Activation of local GABAergic neurons in the AC inhibited responses to the forthcoming natural AS in the AC.
Next, we examined whether HFLS of GABAergic neurons could potentiate their inhibition of neuronal responses to the forthcoming AS in the AC and whether CCK-INs are involved in potentiating their inhibitory outputs toward their target neurons.
In summary, HFLS of local GABAergic neurons potentiated the inhibitory effect of GABAergic neurons on neuronal responses to the forthcoming AS in Vgat-Cre mice but not in Vgat-Cre-CCK-cKO mice. The potentiated inhibition was long lasting and persisted across the observation period of 60 min (Fig. 1J).

HFLS of CCK-INs, but not PV-INs, potentiates sIPSCs in glutamatergic neurons
Earlier studies on cortical inhibitory neuron-related plasticity and behaviors extensively focus on discriminating the distinct roles of PV-IN, SOM-IN, and VIP-IN-induced inhibitory control Pfeffer et al., 2013;Pi et al., 2013;Chen et al., 2017;Yu et al., 2019;Jang et al., 2020) because they account for the majority of neocortical GABAergic neurons (Gonchar, 2008;Whissell et al., 2015) and are easily characterized by selective genetic and histologic labeling. In contrast, cortical CCK-INs constitute a major subclass of GABAergic interneurons but receive less attention because of difficulties isolating CCK-INs.
The above in vivo experiments show that HFLS of GABAergic neurons in Vgat-Cre mice but not in Vgat-Cre-CCK-cKO mice potentiated the inhibition of neuronal activity in the AC. In the next experiment, we performed a patch-clamp recording of pyramidal neurons to examine whether the potentiated inhibition of GABAergic inputs was CCK-IN specific. We targeted CCK-INs and considered PV-INs as a control as PV-INs represent the largest proportion of GABAergic neurons in the cortex and hippocampus and serve to gate perisomatic inhibition (Gonchar, 2008;Whissell et al., 2015;Dudok et al., 2021). Dudok et al. (2021) specifically labeled hippocampal CA1 CCK basket cells Sncg (58 6 17%), but no other inhibitory subtypes using the Sncg-Flp mouse line (Dudok et al., 2021). To unbiasedly label cortical CCK-INs and PV-INs, we combined a Cre recombinasebased genetic approach with the inhibitory neuron-specific intergenic regulatory sequence Dlx5/6 (Whissell et al., 2015), which provides selective genetic access and sufficient labeling in available PV-Cre and CCK-Cre transgenic mouse lines (Taniguchi et al., 2011).

Application of CCK8s and lLFLS to CCK-INs induces iLTP in glutamatergic neurons
Next, we hypothesized that HFLS of CCK-INs triggers the corelease of GABA and CCK that induces the iLTP of their target neurons. At the same time, LFLS with the same number of pulses causes no CCK release and, thus, no iLTP. In this case, the direct application of CCK followed by LFLS could generate iLTP in CCK-INs.

HFLS induces iLTP in CCK1R/2R-KO mice
Next, we aimed to determine which CCK receptor mediates iLTP in CCK-INs. There are two known CCK receptors in the brain, CCK1R and CCK2R. CCK2R is widely distributed throughout the CNS, whereas CCK1R is only found in certain regions, such as the hypothalamus and hippocampus (Honda et al., 1993). We reported that CCK2R mediates the role of entorhinal-cortical CCKs in cortical LTP and the encoding of associative memory (Li et al., 2014;Chen et al., 2019). Thus, we expected that CCK-induced iLTP is mediated by CCK receptors.
We used CCK1R/2R-KO and CCK-KO mice to examine which CCK receptor mediates the contribution of CCK signaling to the iLTP of CCK-INs in brain slice experiments. We performed genotyping confirmation of CCK1R/2R-KO and CCK-KO mouse lines before virus injection and in vitro recording.
We combined two viruses ( Fig. 3A; mDlx-DIO-ChR2-mCherry and mDlx-Cre-helper rAAV9) that both contain mDlx and are expressed only in interneurons. The viruses were injected into the AC of CCK1R/2R-KO and CCK-KO mice.
Immunohistochemical experiments examined whether the combined viruses were expressed in the target GABAergic neurons effectively and precisely. Confocal images showed that almost all infected neurons were GABAergic neurons in both mouse lines ( Fig. 3B; one-way ANOVA with Tukey's post hoc test, N.S.).
We then decided to confirm these iLTPs using the same protocol for in vivo recording in CCK1R/2R-KO mice (Fig. 3G). We examined whether laser activation of GABAergic neurons suppresses neuronal responses in the AC to a forthcoming AS. As expected, HFLS of GABAergic neurons did not reduce the amplitude of LFPs in response to the AS in CCK-KO mice. To our surprise, HFLS of GABAergic neurons induced a distinct / for mean frequency of the AS-triggered firing rate with the laser off or on (DIO-ChETA-eYFPinjected mice, n = 17 units, N = 11 mice; two-way ANOVA with Tukey's post hoc test, ***p , 0.001). E, Multiunit recording in Vgat-Cre mice. Left, Unit response (middle) and mean firing rate (right) of responses to the combined stimulus of the laser and AS before, during, and after HFLS in Vgat-Cre mice. F, Multiunit recording in Vgat-Cre-CCK-cKO mice. Left to right, Unit response and mean firing rate (right) for responses to the combined stimulus of the laser and AS before, during, and after HFLS in Vgat-Cre-CCK-cKO mice. G, Group data for E, F  The bar chart depicts the percentage of mCherry 1 neurons colabeled with GAD67, ChR2, and CCK in CCK-Cre mice or colabeled with PV and ChR2 in PV-Cre mice. C, Schematic drawings show in vitro patch-clamp recording of target PC neurons while delivering a laser pulse to activate infected CCK neurons (top) and PV neurons (bottom). The confocal image depicts the morphology of a representative pyramidal neuron infused with Alexa Flour 488 after patch-clamp recording in CCK-Cre mice. Scale bar, 15 mm. Neuronal firing responses to step currents show the recruited PC with regular spiking. D, Traces of IPSC responses to the laser pulse at 0.1 Hz in brain slices from CCK-Cre and PV-Cre mice before and after HFLS. E, Sampled neuronal responses to the HFLS in PV-Cre and CCK-Cre brain slices. F, Time course of normalized IPSCs before (for 5 min) and after (for 25 min) HFLS in PV-Cre (black, n = 9 neurons; one-way ANOVA with Tukey's post hoc test; N.S.) and CCK-Cre (red, n = 9 neurons; one-way ANOVA with Tukey's post hoc test, ****p , 0.0001; two-way RM ANOVA with Tukey's post hoc test, ####p , 0.0001) mice. G, Schematic drawings show patch-clamp recording targeted at pyramidal neurons while delivering a laser pulse to activate infected neurons and perfusing CCK8s or aCSF. Neuronal responses to step currents were used to confirm that recorded neurons were excitatory with regular spike trains as in C. H, IPSCs in response to the laser pulse in brain slices from CCK-Cre mice perfused with CCK8s or aCSF. I, Time course of normalized IPSCs before (for 5 min) and after (for 25 min) LFLS in brain slices from CCK-Cre mice perfused with aCSF (blue, n = 8 neurons; one-way ANOVA with Tukey's post hoc test, N.S., not significant) or CCK8s (red, n = 8 neurons; one-way ANOVA with Tukey's post hoc test, ****p , 0.0001; two-way RM ANOVA, post hoc with Tukey HSD, ####p , 0.0001). Data are expressed as mean 6 SEM.
These results indicate that CCK-enabled iLTP is likely mediated by a novel receptor other than CCK1R or CCK2R. E, Sampled neuronal responses to HFLS in CCK1R/2R-KO and CCK-KO mice. F, Time course of normalized IPSCs before and after (for 25 min) HFLS in CCK-KO (black, n = 9 neurons; one-way ANOVA with Tukey's post hoc test, N.S., not significant) and CCK1R/2R-KO mice (green, n = 9 neurons; one-way ANOVA with Tukey's post hoc test, ****p , 0.0001; two-way RM ANOVA with Tukey's post hoc test, ####p , 0.0001). G, Schematic illustration of the setup for in vivo recordings with laser stimulation in the AC and a natural AS (a noise burst; SOM, PV neuron, PC) in CCK1R/2R-KO (left) and CCK-KO (right) mice. Bottom, Example waveforms from the two groups. H, Normalized LFP response amplitudes to the AS with a preceding laser pulse before and after HFLS in CCK1R/2R-KO (green, n = 7 recording sites, N = 5 mice) and CCK-KO (black, n = 8 recording sites, N = 6 mice; two-way RM ANOVA with Tukey's post hoc test, ****p , 0.0001) mice. Data are expressed as mean 6 SEM.
The downstream signals of many GPCRs are unclear, especially for .100 orphan GPCRs . Bioinformatics prediction is the most efficient method of finding GPCR-ligand pairs and hence was adopted in our study to search for novel CCK receptors in the brain. Combining cell-based assays with bioinformatics prediction has enabled the identification of many GPCR-ligand pairs, such as bombesin receptor 3 (BB3)-neuromedin B, BB3-gastrin-releasing peptide, GPR15-GPR15L 47-57 , GPR68-Osteocrin 33-55 , and GABA B R1a-sAPPa (Foster et al., 2019;Rice et al., 2019). In addition, loss-of-function and gainof-function studies coupled with histology verification are very important for exploring the physiological functions of novel GPCRs.
Recently, highly accurate protein 2D alignment or 3D structure prediction has facilitated the development of new drugs targeting GPCRs (Insel et al., 2019;Yang et al., 2021). The online alignment of the 2D protein sequence (Sievers et al., 2011) and prediction of the 3D structure by AlphaFold2 or ColabFold systems (Senior et al., 2020;Du et al., 2021;Tunyasuvunakool et al., 2021;Mirdita et al., 2022;Varadi et al., 2022) enables us to map CCK receptors rapidly and comprehensively. We speculated that a new CCK receptor mediates CCK8s-induced iLTP in the mouse AC, which is probably a GPCR similar to CCK1R/2R. The 2D sequences of CCK receptors should be evolutionarily homologous. We predicted the secondary structure of amino acid sequences of selected brain GPCRs using the free online software NetSurfP version 1.1 (Petersen et al., 2009). The binding sites of all GPCR secondary structures (extramembrane) were selected based on the CCK binding domains of CCK1R and CCK2R, and the GPCRs were compared with the two CCK receptors based on hamming distance. We listed the GPCRs with the highest scores (Fig. 4A) as probable candidates for CCK receptors.
To further evaluate which of these GPCR candidates is a novel CCK receptor, we established a cell surface binding assay according to previous reports (De Wit et al., 2013;Rice et al., 2019;Fig. 4B). In this system, the CDS of candidate GPCRs, as well as CCK2R with an N-terminal Flag tag, were cloned into pCDNA3.1(1) to transfect HEK293T cells (Fig. 4B-D). We also synthesized a series of HA-(« -Ahx) 2 -CCK variant probes, including CCK4, CCK8s, nonsulfated CCK8 (CCK8ns), and control HA-(« -Ahx) 2 , which have been detected in the body with different specificity for CCK1R/2R.
As CCK8s is the main form of CCK in the brain (Dockray et al., 1978;Agersnap et al., 2016), we applied a cell surface binding assay with HA-tagged CCK8s for the first-round screening of GPCR candidates with high scores, including Flag-tagged GPR173, HTR2C, HTR1F, HTR2B, HTR1E, HTR1B, and NPY5R (Fig. 4B,C). We demonstrated that HA-tagged CCK4, HA-tagged CCK8ns, and HA-tagged CCK8s colocalized with Flag-tagged CCK2R, with a significantly larger ratio of CCK ligand HA-tag signal to CCK2R Flag signal (F anti-HA /F anti-Flag ) than that of the HA-(« -Ahx) 2 control group, suggesting that our cell surface binding assay was applicable for characterizing the binding of CCK ligands and receptors.
CCK-2R and GPR173 bound to CCK8s, whereas other GPCR candidates did not (Fig. 4B-D). Thus, detailed ligand specificity analysis was performed using HA-tagged CCK4/CCK8ns/CCK8s probes, in which HTR1B-expressing cells served as negative/ background control. Flag-tagged GPR173 could only bind to HA-tagged CCK8 but not HA-tagged CCK4 or CCK8ns (Fig. 4B), indicating that CCK8s is a specific ligand of GPR173. No binding of HA-tagged CCK4/CCK8ns/CCK8s with Flag-tagged HTR1B was detected. To further verify the binding between GPR173 and CCK8s, we used a competitive cell surface binding procedure, in which Flag-tagged GPR173-expressing HEK293T cells were incubated with a CCK8s and HA-tagged CCK8s (1:1) mixture. We found that CCK8s significantly blocked the HA-tag signals from binding HA-tagged CCK8s (Fig. 4B-D). Together, we conclude that GPR173 is a novel CCK receptor, and CCK8s is a ligand of GPR173.
GPR173 is located at CCK-GABAergic synapses in the AC The above evidence confirmed that GPR173 is a novel CCK receptor. Here, we performed histochemical analysis and used another bioinformatics prediction algorithm to verify whether GPR173 or another novel CCK receptor mediates HFLS-induced iLTP.
In the bioinformatics prediction algorithm, we used the Clustal Omega program (Sievers et al., 2011) to extract homologous information for 79 orphan receptors from class A GPCRs aligned with the two known CCK receptors. The percentage identity correlation score defines the quantitative correlation estimation between two sets of sequences (Raghava and Barton, 2006). According to the percentage identity correlation score among 79 orphan receptors and CCK1R/2R, we selected top-scored orphan receptors normalized by CCK1R and CCK2R (Fig. 5A). Interestingly, GPR83, which was recently reported as a novel CCK receptor (Mack et al., 2022), was also among the five top-scored candidates (Fig. 5A).
We also checked whether GPR173 colocalizes with GABA A R in mDlx-DIO-ChR2-mCherry-injected CCK-Cre mice using super-resolution imaging with a STORM confocal microscope (Fig. 5E). We found that both GPR173 and GABA A R appeared within mCherry-labeled CCK-GABAergic synapses, and GPR173 and GABA A R also nearly colocalized (Fig. 5E). To determine the co-occurrence and correlation coefficients of GPR173, GABA A R, and mCherry-labeled CCK-GABAergic synapses, we further analyzed data from super-resolution images using PCC and MOC, which are common metrics for measuring the predictability of colocalization (Aaron et al., 2018;Fig. 5E). The numerical values of PCC and MOC were .0.78 across six clusters, suggesting that GPR173 is located in GABAergic synapses and near GABA A Rs.
To further confirm that CCK-GABAergic synapses directly contact excitatory pyramidal neurons, we counted numbers of colocalized GPR173 and CCK-INs contacts on CaMKII 1 neurons ( Fig. 5G; n = 49 neurons, 5.69 6 0.38) in cortical slices from CCK-Cre mice (as described in Fig. 5B). All these data suggest that GPR173 is located at CCK-GABAergic synapses and might be involved in CCK-dependent HFLS-induced iLTP. In the present study, we cannot exclude the possibility that CCK-IN-induced iLTP is restricted to the CCK postsynaptic area without affecting neighboring PV synapses. It would be worth investigating whether this iLTP is homosynaptic or heterosynaptic. . Bioinformatics and cell surface binding assay screening for a novel CCK receptor. A, Bar chart showing the highest similarity scores between GPCRs and known CCK receptors (CCK1R and CCK2R) considering the secondary structure in amino acid sequences, including six GPCRs for 5-hydroxytryptamine (serotonin; HTR2C, HTR1F, HTR2B, HTR1E, HTR1B, and HTR1D), an orphan receptor (GPR173), neuropeptide Y receptor Y5 (NPY5R), and adrenergic receptor beta 1 (ADRB1). B-D, Schematic of cell surface binding assay for Flag-tagged GPCRs with negative control (HA-(« -Ahx) 2 ) or HA-(« -Ahx) 2 -CCK variants (HA-CCK4, HA-CCK8ns, and HA-CCK8s). Confocal images (B, top; scale bar, 10 mm) and quantification of fluorescence intensity ratio (F anti-HA /F anti-Flag ; B, D, bottom) in the cell surface binding assay for Flag-CCK2R, Flag-GPR173, Flag-HTR1B, and five other Flag-GPCRs as shown in C. The number of total cells from three independent experiments is defined as n; n = 33-40, one-way ANOVA with Tukey's post hoc test or unpaired Student's t test, **p , 0.01, ****p , 0.0001, N.S., not significant. Data are expressed as mean 6 SEM. CCK8s triggers intracellular Ca 21 mobilization through GPR173 CCK1R and CCK2R could couple to Gq protein, through which CCK1R/2Rs trigger intracellular Ca 21 release from the endoplasmic reticulum after their activation (Dunlop et al., 1996;Dufresne et al., 2006). CCK8s, as a potent but nonselective agonist of both CCK1R and CCK2R (Berna et al., 2007), mainly works via the Gq-PLC-IP 3 -Ca 21 pathway (Dunlop et al., 1996;Wu et al., 1997). We hypothesized that the novel CCK receptor should also trigger intracellular Ca 21 mobilization through this pathway on binding to CCK8s. Thus, we built a cell-based Ca 21 imaging assay by constructing stable monoclonal GPCR transgenic CHO cell lines for CHO-GPR173, CHO-CCK1R, and CHO-CCK2R.
As a low endogenous level of CCK1R/2Rs may be expressed in CHO-GPR173 cells, the CCK2R-specific agonist CCK4 (Lin et al., 1989) and CCK1R-specific agonist A-71 623 (Lin et al., 1991) were applied to exclude false-positive signals. As expected, CHO-CCK2R and CHO-CCK1R cells responded to CCK4 and A-71 623, respectively, in a concentration-dependent manner, but neither could induce Ca 21 release in CHO-GPR173 cells (Fig. 6D, E). We then tried to knock down the expression of GPR173 by applying shRNA (Gpr173) in CHO-GPR173 cells (Fig. 6F). The Ca 21 signal was downregulated by .50% after the mRNA level of GPR173 was knocked down by .50% (Fig. 6G). GPR173, also known as SREB3, is highly evolutionarily conserved and predominantly expressed in the CNS (Matsumoto et al., 2005;Regard et al., 2008). The endogenous ligands and physiological functions of GPR173 have not properly and directly been determined in the brain. A previous study of the phoenixin (PNX)/GPR173 system illustrates that PNX is essential for regulating the mRNA of GPR173 in the pituitary (Treen et al., 2016). However, from our cell-based assays, the CCK ligand CCK8s binds to GPR173 with nM potency. In contrast, PNX did not directly trigger an immediate Ca 21 response (Fig. 6H) or b -arrestin recruitment (Vandevoorde et al., 2018). Thus, PNX may modulate GPR173 activity or expression through an unknown pathway that needs further investigation.
These results indicate that the CCK8s-induced Ca 21 response in CHO-GPR173 cells was mediated by GPR173, again supporting that GPR173 is a novel CCK receptor.
In addition to the cell surface binding and Ca 21 imaging assays, we also applied a b -arrestin2 recruitment assay (PRESTO-Tango assay; Kroeze et al., 2015) to verify whether GPR173 is a CCK receptor. However, no b -arrestin2 recruitment was found for GPR173 after incubation with CCK8s (Fig. 6L). Consequently, we coexpressed b -arrestin1-conjugated TEV protease in the b -arrestin2 recruitment assay to detect whether GPR173 could recruit b -arrestins. We named this method the b -arrestin1/2 recruitment assay (Fig. 6I). We found that the b -arrestin1/2 recruitment signal for CCK1R was much higher than that in the b -arrestin2 assay (Fig. 6J), which is in line with previous reports that CCK1R could recruit b -arrestin1 (Ning et al., 2015). Meanwhile, the b -arrestin1/2 recruitment efficiency of CCK2R was far more than that in the b -arrestin2 recruitment assay (Fig. 6K), indicating that our modified b -arrestin recruitment system is reliable and more efficient. Next, we checked the dose-dependent response of CCK8s-induced b -arrestin recruitment for GPR173. We found that GPR173 responded to CCK8s in the b -arrestin1/2 recruitment assay (Fig. 6L).
In summary, CCK8s-induced b -arrestin recruitment further supports that GPR173 is likely a novel CCK receptor.
In summary, this evidence further supports that GPR173, a novel CCK receptor, mediates the CCK signal from CCK-INs and induces iLTP in their synapses. / DAPI (n = 21 cells). E, Super-resolution image of colocalized GPR173 with CCK-GABAergic synapses, GABA A R with CCK-GABAergic synapses, and GABA A R and GPR173 (left). Scale bar, 1 mm. The values for PCC and MOC indicate the colocalization possibility of mCherry with GPR173, mCherry with GABA A R, and GABA A R with GPR173. F, Immunochemistry images of costaining of GPR173 with CaMKII (top) or GAD67 (bottom) in C57BL/6J mice. Scale bar, 50 mm. Group data from colocalization analysis of GPR173 with CaMKII (n = 11 sections, N = 3 mice) or GAD 67 (n = 10 sections, N = 3 mice). G, Immunochemistry images for colocalized GPR173 with CCK-GABAergic synapses contacting pyramidal cells and box plot showing numbers of colocalized GPR173 and CCK-GABAergic contacts per pyramidal cell (n = 49 neurons, 5.69 6 0.38). Scale bar, 5 mm. Data are expressed as mean 6 SEM. Relative fluorescence unit (RFU) is defined as the ratio of RFU before and 30 s after adding CCK8s/HHBS (unpaired Student's t test, *p , 0.05, ****p , 0.0001, N.S., not significant). I, Illustration of the b -arrestin1/2 recruitment assay design. J, Dose-dependent response of CCK8s-induced b -arrestin recruitment to CCK1Rs determined by the b -arrestin2 recruitment and b -arrestin1/2 recruitment assays. The two control groups were without GPCR plasmid transfection in HTLA cells. K, L, Dose-dependent response of CCK8s-induced b -arrestin recruitment to CCK2Rs (K) and GPR173 (L) determined by the b -arrestin2 recruitment and b -arrestin1/2 recruitment assays (at least n = 3 independent experiments; one-way ANOVA with Tukey's post hoc test or unpaired Student's t test, ****p , 0.0001). Data are expressed as mean 6 SEM.

Discussion
Because of the complexity of inhibitory neurons and connections, heterogeneous forms of inhibitory plasticity exist. Previous investigators proposed mechanisms for enhanced inhibitory control expressed at either the presynaptic or postsynaptic level. Different mechanisms of inhibitory plasticity at the presynaptic level that have been proposed include the release of more GABA transmitters (Caillard et al., 1999;Fiszman et al., 2005;Nugent et al., 2007), increased PV expression (Patz et al., 2004), and a GABAergic inhibition-induced decrease in glutamate release (Pan et al., 2009). iLTP is induced by postsynaptic activation of VGCCs (Kang et al., 1998;Caillard et al., 1999;Udakis et al., 2020). VGCCs provide a Ca 21 source for activating CaMKII (Udakis et al., 2020), which induces GABA A R phosphorylation and leads to iLTP (Petrini et al., 2014;He et al., 2015;Chiu et al., 2018). A study on awake mice identified a group of GABAergic neurons that burst or fire vigorously during rest and sharp-wave ripples and stay silent during locomotion and theta states (Szabo et al., 2022). CCK-INs are most active when the animal is at rest, whereas PV-INs remain silent (Dudok et al., 2021). However, most of these studies focus on inhibition-regulating behaviors depending on the hippocampus. More detailed mechanisms of iLTP from in vivo or long-term behavioral experiments remain elusive. Excitatory input arrives at the cell together with an inhibitory counterpart when an external stimulus activates the local cortex, which is normally recognized as the foundation of balanced cortical circuits (Galindo-Leon et al., 2009;Vogels et al., 2011;Alluri et al., 2016). We found that high-frequency activation of GABAergic neurons potentiated their long-term inhibition toward their target neurons and enhanced the general inhibition of the surrounding region, as reflected in the integrated neuronal responses to the forthcoming AS (Fig. 1). This iLTP in a the brain of a mature animal is critical for imbalanced excitation-and inhibition-induced brain disorders in adults (Vogels et al., 2011).
Considering the diverse electrophysiological, molecular, and structural features of GABAergic neurons, functional and behavioral correlates of this diversity are to be clarified accordingly. For example, PV-INs take leading control of the fast and powerful inhibitory effect on local neural activity, which makes them vital for the synchronization of spikes and synchronous gamma (30-80 Hz) oscillations Chen et al., 2017;Jang et al., 2020). Stronger synchronization of PV-IN activity acts as a functional unit in the local medial prefrontal cortex, promoting goal-directed behavior (Kim et al., 2016). SOM-INs inhibit distal dendrites of excitatory neurons, causing them to act as key regulators of whisker movements in the somatosensory cortex (Yu et al., 2019) and the acquisition of motor skills in the motor cortex . Dendritic iLTP of SOM-IN synapses is driven by Ca 21 influx through NMDARs, whereas inputs from PV-INs and VIP-INs are unaffected (Chiu et al., 2018). These findings indicate the possibility of circuit-specific plasticity of GABAergic neurons.
In the visual cortex, high-frequency electrical stimulus trains (50 Hz) induce GABA A R-dependent LTP of inhibitory postsynaptic potentials of pyramidal neurons in developing rats (Komatsu, 1994). HFS of the subthalamic nucleus increases extracellular striatal GABA in hemiparkinsonian rats, which may benefit patients suffering from severe parkinsonism (Bruet et al., Figure 7. Devazepide as a GPR173 antagonist could block HFS-induced iLTP. A, The dose-dependent response curve of CHO-GPR173 cells activated by 10 nM CCK8s after incubation with antagonists for 30 min (at least n = 3 independent experiments). B, Injection of rAAV9-mDlx-DIO-ChR2-mCherry into CCK-Cre and PV-Cre mice. C, Schematic drawing shows in vitro patch-clamp recording from a target PC neuron while delivering a laser pulse to activate infected CCK neurons (top). D, Traces of IPSC responses to HFLS in brain slices from CCK-ires-Cre mice before and after HFLS (red) or devazepide 1 HFLS (black). E, Time course of normalized IPSCs before (for 5 min) and after (for 25 min) HFLS in CCK-ires-Cre mice or after (for 25 min) devazepide plus HFLS in CCK-Cre mice (black, n = 9 neurons; one-way ANOVA with Tukey's post hoc test, N.S. not significant; two-way RM ANOVA with Tukey's post hoc test, ****p , 0.0001). Data are expressed as mean 6 SEM.